List of variants in gene SYN1 reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_006950.3(SYN1):c.1107C>T (p.Ile369=)	rs150248483	0.00107
NM_006950.3(SYN1):c.1325T>C (p.Leu442Pro)	rs375440874	0.00058
NM_006950.3(SYN1):c.1615G>A (p.Gly539Ser)	rs794727076	0.00058
NM_006950.3(SYN1):c.1569G>A (p.Ala523=)	rs587781185	0.00022
NM_006950.3(SYN1):c.371C>T (p.Thr124Ile)	rs1339768860	0.00004
NM_006950.3(SYN1):c.316G>T (p.Ala106Ser)	rs794726957	0.00001
NM_006950.3(SYN1):c.138C>G (p.Pro46=)	rs794726958
NM_006950.3(SYN1):c.1614A>G (p.Gly538=)	rs794727075
NM_006950.3(SYN1):c.1964C>T (p.Pro655Leu)	rs1333198986
NM_006950.3(SYN1):c.377+15C>T	rs1347721908

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